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Structure of 7749-47-5
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2-Amino-4-methoxy-6-methylpyrimidine features a pyrimidine core functionalized with amino, methoxy, and methyl groups at positions 2, 4, and 6 respectively. This electron-rich scaffold serves as a key building block in medicinal chemistry, particularly for kinase inhibitors and antiviral agents. The methoxy and methyl substituents enhance solubility and metabolic stability, while the amino group enables facile derivatization.
2-Amino-4-methoxy-6-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling efficient access to pyrimidine-based scaffolds through standard coupling and functionalization reactions. Its complementary amino and methoxy groups offer orthogonal reactivity for selective derivatization, while the methyl substituent enhances metabolic stability. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for both small-scale lead optimization and scalable synthesis workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P405-P501
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Lot numbers can be found on the outside label of a product: